Fabricating method of non-volatile memory cell

ABSTRACT

A super-silicon-rich oxide (SSRO) non-volatile memory cell includes a gate conductive layer on a substrate, a source/drain in the substrate at respective sides of the gate conductive layer, a tunneling dielectric layer between the gate conductive layer and the substrate, a SSRO layer serving as a charge trapping layer between the gate conductive layer and the tunneling dielectric layer, and an upper-dielectric layer between the gate conductive layer and the SSRO layer.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a memory cell and a fabricating method thereof. More particularly, the present invention relates to a non-volatile memory and a fabricating method thereof.

2. Description of Related Art

Recently, demands on electrical consumers are increasing. Most of the electrical consumers including digital cameras, MP3 players, laptop computers and personal digital assistants (PDAs) require read-only memories (ROMs) for storing a great deal of data. Since information or the data stored in the ROM are not volatiled even though the power is off, the ROM is also called a non-volatile memory. The most common ROM goes to an electrically erasable programmable ROM (EEPROM) which is not only capable of reading and writing but also allows multiple programming and erasing operations.

The typical EEPROM adopts doped polysilicon as a control gate and a floating gate. During a programming operation performed on the EEPROM, electrons injected into the floating gate may be distributed over the whole doped polysilicon floating gate layer in a uniform manner. However, when there are defects in a tunneling oxide layer under the doped polysilicon floating gate layer, current leakage of the device may occur, and the reliability of the device is adversely affected.

Currently, the issue of current leakage occurring in the EEPROM may be resolved with use of a certain device. This device employs a charge trapping layer as a replacement for the doped polysilicon floating gate layer. Since the charge trapping layer is made of a material characterized by capturing the electrons, the electrons injected into the charge trapping layer are not uniformly distributed over the charge trapping layer. Instead, the electrons with a Gaussian distribution property are collected in partial areas of the charge trapping layer. Since the electrons injected into the charge trapping layer are merely concentrated in the partial areas, said charge trapping layer has little sensitivity to the defects of the tunneling oxide layer, thus lessening the current leakage of the device. Typically, the material of the charge trapping layer is silicon nitride. The charge trapping layer made of silicon nitride is normally sandwiched between a top silicon oxide layer and a bottom silicon oxide layer to form a stacked gate structure including a silicon oxide/silicon nitride/silicon oxide (ONO) composite dielectric layer. The EEPROM having said stacked gate structure is frequently referred to as a silicon nitride ROM. However, the number of the charges captured by the charge trapping layer made of silicon nitride and the capturing speed of the charge trapping layer are not quite impressive.

SUMMARY OF THE INVENTION

The present invention is directed to a non-volatile memory cell which is able to increase the number of charges captured by a charge trapping layer.

The present invention is further directed to a non-volatile memory cell which is capable of increasing the capturing speed achieved by the charge trapping layer.

The present invention is further directed to a fabricating method of a non-volatile memory cell. Said fabricating method may resolve the issues of few numbers of charges captured by a charge trapping layer and of low capturing speed of the charge trapping layer.

The present invention provides a super-silicon-rich oxide (SSRO) non-volatile memory cell including a substrate, a gate conductive layer, a source/drain, a tunneling dielectric layer, a SSRO layer, and an upper-dielectric layer. The gate conductive layer is disposed on the substrate. The source/drain is disposed in the substrate at respective sides of the gate conductive layer. The tunneling dielectric layer is disposed between the gate conductive layer and the substrate. The SSRO layer serving as a charge trapping layer is disposed between the gate conductive layer and the tunneling dielectric layer. The upper-dielectric layer is disposed between the gate conductive layer and the SSRO layer.

According to an embodiment of the present invention, a refractive index at 248 nm wave length of the SSRO layer ranges from 1.7 to 2.

According to an embodiment of the present invention, the refractive index at 248 nm wave length of the SSRO layer is 1.7.

According to an embodiment of the present invention, a material of the upper-dielectric layer is silicon oxide.

According to an embodiment of the present invention, a thickness of the SSRO layer ranges from 80 angstroms to 120 angstroms.

According to an embodiment of the present invention, a thickness of the upper-dielectric layer ranges from 70 angstroms to 110 angstroms.

According to an embodiment of the present invention, the tunneling dielectric layer is a tunneling oxide layer and a thickness of the tunneling oxide layer ranges from 40 angstroms to 50 angstroms.

According to an embodiment of the present invention, the tunneling dielectric layer comprises a bottom oxide layer, a nitride layer and a top oxide layer from bottom to top formed between the SSRO layer and the substrate.

According to an embodiment of the present invention, a thickness of the bottom oxide layer is less than 20 angstroms.

According to an embodiment of the present invention, a thickness of the bottom oxide layer ranges from 5 angstroms to 20 angstroms.

According to an embodiment of the present invention, a thickness of the bottom oxide layer is less than 15 angstroms.

According to an embodiment of the present invention, a thickness of the nitride layer is less than 20 angstroms.

According to an embodiment of the present invention, a thickness of the nitride layer ranges from 10 angstroms to 20 angstroms.

According to an embodiment of the present invention, a thickness of the top oxide layer is less than 20 angstroms.

According to an embodiment of the present invention, a thickness of the top oxide layer ranges from 15 angstroms to 20 angstroms.

The present invention further provides a cluster non-volatile memory cell including a substrate, a gate conductive layer, a source/drain, a tunneling dielectric layer, a charge trapping layer, and an upper-dielectric layer. The gate conductive layer is disposed on the substrate. The source/drain is disposed in the substrate at respective sides of the gate conductive layer. The tunneling dielectric layer is disposed between the gate conductive layer and the substrate. The charge trapping layer is disposed between the gate conductive layer and the tunneling dielectric layer. Besides, the charge trapping layer is an insulating layer, and a plurality of clusters are disposed in the insulating layer. The upper-dielectric layer is disposed between the gate conductive layer and the charge trapping layer.

According to an embodiment of the present invention, a material of the insulating layer includes silicon oxide, and the clusters are made of silicon atoms.

According to an embodiment of the present invention, a refractive index at 248 nm wave length of the charge trapping layer ranges from 1.7 to 2.

According to an embodiment of the present invention, the refractive index at 248 nm wave length of the charge trapping layer is 1.7.

According to an embodiment of the present invention, a material of the upper-dielectric layer is silicon oxide.

According to an embodiment of the present invention, a thickness of the SSRO layer ranges from 80 angstroms to 120 angstroms.

According to an embodiment of the present invention, a thickness of the upper-dielectric layer ranges from 70 angstroms to 110 angstroms.

According to an embodiment of the present invention, the tunneling dielectric layer is a tunneling oxide layer and a thickness of the tunneling oxide layer ranges from 40 angstroms to 50 angstroms.

According to an embodiment of the present invention, the tunneling dielectric layer comprises a bottom oxide layer, a nitride layer and a top oxide layer from bottom to top formed between the SSRO layer and the substrate.

According to an embodiment of the present invention, a thickness of the bottom oxide layer is less than 20 angstroms.

According to an embodiment of the present invention, a thickness of the bottom oxide layer ranges from 5 angstroms to 20 angstroms.

According to an embodiment of the present invention, a thickness of the bottom oxide layer is less than 15 angstroms.

According to an embodiment of the present invention, a thickness of the nitride layer is less than 20 angstroms.

According to an embodiment of the present invention, a thickness of the nitride layer ranges from 10 angstroms to 20 angstroms.

According to an embodiment of the present invention, a thickness of the top oxide layer is less than 20 angstroms.

According to an embodiment of the present invention, a thickness of the top oxide layer ranges from 15 to 20 angstroms.

The present invention further provides a fabricating method of a SSRO non-volatile memory cell. In said fabricating method, a source/drain is firstly formed in a substrate, and a tunneling dielectric layer is formed on the substrate. Next, a SSRO layer serving as a charge trapping layer is formed on the tunneling dielectric layer. Thereafter, an upper-dielectric layer is formed on the SSRO layer, and finally a gate conductive layer is formed on the upper-dielectric layer.

According to an embodiment of the present invention, a method of forming the SSRO layer includes forming a silicon oxide layer on the tunneling dielectric layer and simultaneously forming a plurality of clusters of silicon atoms in the silicon oxide layer.

According to an embodiment of the present invention, a method of forming the SSRO layer includes implementing a plasma enhanced chemical vapor deposition (PECVD) process.

According to an embodiment of the present invention, a reactive gas which is flowed during the implementation of the PECVD process includes N₂O and SiH₄ having a flow ratio between 0.5 and 1.

According to an embodiment of the present invention, a flow rate of N₂O during the implementation of the PECVD process ranges from 80 sccm to 100 sccm.

According to an embodiment of the present invention, a flow rate of SiH₄ during the implementation of the PECVD process ranges from 160 sccm to 170 sccm.

According to an embodiment of the present invention, a temperature during the implementation of the PECVD process ranges from 350° C. to 450° C.

According to an embodiment of the present invention, a pressure during the implementation of the PECVD process ranges from 2.5 torr to 8.5 torr.

According to an embodiment of the present invention, a high-frequency power provided through the implementation of the PECVD process ranges from 100 W to 130 W.

According to an embodiment of the present invention, a thickness of the SSRO layer ranges from 80 angstroms to 120 angstroms.

According to an embodiment of the present invention, a refractive index at 248 nm wave length of the charge trapping layer ranges from 1.7 to 2.

According to an embodiment of the present invention, a material of the upper-dielectric layer is silicon oxide.

According to an embodiment of the present invention, the step of forming the tunneling dielectric layer including forming a tunneling oxide layer on the substrate.

According to an embodiment of the present invention, the step of forming the tunneling dielectric layer comprises forming a bottom oxide layer, a nitride layer and a top oxide layer from bottom to top on the substrate.

In the present invention, the cluster-containing oxide layer such as the SSRO layer is utilized as the charge trapping layer of the non-volatile memory cell. Thereby, the number of the charges captured by the charge trapping layer of the non-volatile memory cell can be increased, and the capturing speed achieved by the charge trapping layer can be raised.

In order to make the aforementioned and other objects, features and advantages of the present invention more comprehensible, several embodiments accompanied with figures are described in detail below.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a cross-sectional schematic view illustrating a SSRO non-volatile memory cell according to an embodiment of the present invention.

FIG. 1B is a cross-sectional schematic view illustrating a SSRO non-volatile memory cell according to another embodiment of the present invention.

FIG. 2 is an enlarged partial schematic view of the SSRO layer in FIG. 1.

FIGS. 3A through 3E are cross-sectional schematic views illustrating a process of fabricating a SSRO non-volatile memory cell according to an embodiment of the present invention.

FIG. 4 is a curve diagram illustrating experimental results with respect to a relation between a programming (PGM) time and a variation of a corresponding threshold voltage (ΔV_(T)) in a conventional silicon nitride device and that in a SSRO device according to the present invention.

FIG. 5 is a curve diagram illustrating the experimental results with respect to the relation between the PGM time and the corresponding ΔV_(T) in a silicon-rich oxide (SRO) device and that of the SSRO device according to the present invention.

DESCRIPTION OF EMBODIMENTS

Please refer to FIGS. 1A and 1B which are a cross-sectional schematic view illustrating a SSRO non-volatile memory cell according to an embodiment of the present invention, respectively.

Referring to FIGS. 1A and 1B, the non-volatile memory cell includes a substrate 100, doped regions 102, a tunneling dielectric layer 104, a SSRO layer 106, an upper-dielectric layer 108, and a gate conductive layer 110. The substrate 100 may be, for example, a silicon substrate. Dopants in the substrate 100 include N-type dopants or P-type dopants. The doped regions 102 serve as a source/drain, and the dopants therein can be classified into the N-type dopants or the P-type dopants. In one embodiment, the dopants in the substrate 100 are the P-type dopants, while the dopants in the doped regions 102 are the N-type dopants. Contrarily, in another embodiment, the dopants in the substrate 100 are the N-type dopants, while the dopants in the doped regions 102 are the P-type dopants.

The tunneling dielectric layer 104 is disposed on the substrate 100 between the doped regions 102. In an embodiment, the tunneling dielectric layer 104 is a tunneling oxide layer, for example, a silicon oxide layer, and a thickness thereof ranges from 40 angstroms to 50 angstroms, for example, as shown in FIG. 1A. In another embodiment, tunneling dielectric layer 104 comprises a bottom oxide layer 104 a, a nitride layer 104 b and a top oxide layer 104 c from bottom to top formed on the substrate 100 as shown in FIG. 1B. The materials of the bottom oxide layer 104 a and the top oxide layer 104 c include silicon oxide, for example. The material of the nitride layer 104 b includes silicon nitride. In an embodiment, a thickness of the bottom oxide layer 104 a is less than 20 angstroms. In the other embodiment, a thickness of the bottom oxide layer 104 a ranges from 5 angstroms to 20 angstroms. In another embodiment, a thickness of the bottom oxide layer 104 a is less than 150 angstroms. In an embodiment, a thickness of the nitride layer 104 b is less than 20 angstroms. In an embodiment, thickness of the nitride layer 104 b ranges from 10 to 20 angstroms. In an embodiment, a thickness of the top oxide layer 104 c ranges from 15 to 20 angstroms. The following descriptions use a tunneling dielectric layer 104 constituted of a single layer as shown in FIG. 1A.

The SSRO layer 106 serving as a charge trapping layer is disposed on the tunneling dielectric layer 104. For better demonstration, an enlarged partial schematic view of the SSRO layer 106 is depicted in FIG. 2. Referring to FIG. 2, the SSRO layer 106 includes an oxide layer 200 having a plurality of cluster 202 of silicon atoms. As the memory cell is programmed, charges can be stored in the cluster 202 of the silicon atoms. In one embodiment, a refractive index at 248 nm wave length of the SSRO layer 106 ranges from 1.7 to 2. In another embodiment, the refractive index at 248 nm wave length of the SSRO layer 106 is 1.7. A thickness of the SSRO layer 106 ranges from 80 angstroms to 120 angstroms, for example.

The upper-dielectric layer 108 is disposed on the SSRO layer 106. In an embodiment, a material of the upper-dielectric layer 108 is silicon oxide, and a thickness thereof ranges from 70 angstroms to 110 angstroms. The gate conductive layer 110 is disposed on the upper-dielectric layer 108. In an embodiment, the gate conductive layer 110 is a doped polysilicon layer. However, in another embodiment, the gate conductive layer 110 is constructed by a doped polysilicon layer and a silicide layer.

FIGS. 3A through 3E are cross-sectional schematic views illustrating a process of fabricating a SSRO non-volatile memory cell according to an embodiment of the present invention.

First, referring to FIG. 3A, a substrate 100, for example, a silicon substrate, is provided. Dopants in the silicon substrate 100 include N-type dopants or P-type dopants. Two doped regions 102 are then formed on the substrate 100 as a source/drain. A method of forming the doped regions 102 may be a thermal diffusion method or an ion implantation method, for example. The dopants in the doped regions 102 may be the N-type dopants or the P-type dopants. In an embodiment, the dopants in the substrate 100 are the P-type dopants, while the dopants in the doped regions 102 are the N-type dopants. Contrarily, in another embodiment, the dopants in the substrate 100 are the N-type dopants, while the dopants in the doped regions 102 are the P-type dopants.

Then, a tunneling dielectric layer 104 is formed on the substrate 100. In an embodiment, the tunneling dielectric layer 104 is a tunneling oxide layer as shown in FIG. 3A. The tunneling oxide layer is made of, for example, silicon oxide, and is formed by performing a thermal oxidation process. A thickness of the tunneling dielectric layer 104 ranges from 40 angstroms to 50 angstroms.

Referring to FIG. 3AA, in another embodiment, the tunneling dielectric layer 104 comprises a bottom oxide layer 104 a, a nitride layer 104 b and a top oxide layer 104 c from bottom to top formed on the substrate 100. The bottom oxide layer 104 a is formed by a thermal oxidation process, for example. The nitride layer 104 b is form by a CVD process, for example. The top oxide layer 104 c is formed by a CVD process, for example. The following processes are described using a tunneling dielectric layer 104 constituted of a single layer as shown in FIG. 3A.

After that, referring to FIG. 3B, a SSRO layer 106 is formed on the tunneling oxide layer 104. The enlarged partial schematic view of the SSRO layer 106 is depicted in FIG. 2. Referring to FIG. 2, the SSRO layer 106 includes an oxide layer 200 having a plurality of cluster 202 of silicon atoms. As the memory cell is programmed, charges can be stored in the cluster 202 of the silicon atoms. In an embodiment, a refractive index at 248 nm wave length of the SSRO layer 106 ranges from 1.7 to 2. In another embodiment, the refractive index at 248 nm wave length of the SSRO layer 106 is 1.7. Besides, in one embodiment, a thickness of the SSRO layer 106 ranges from 80 angstroms to 120 angstroms, and the SSRO layer 106 is formed by performing a PECVD process, such that the silicon oxide layer 200 is formed, and a plurality of the cluster 202 of the silicon atoms is simultaneously formed in the silicon oxide layer 200. In an embodiment, the SSRO layer 106 is formed by performing the PECVD process at a temperature ranging from 350° C. to 450° C., a pressure ranging from 2.5 torr to 8.5 torr and a high-frequency power ranges from 100 W to 130 W. The reaction gas for implementing the PECVD process includes N₂O and SiH₄. A flow ratio of N₂O to SiH₄ is between 0.5 and 1. A flow rate of N₂O ranges from 80 sccm to 100 sccm, while a flow rate of SiH₄ ranges from 160 sccm to 170 sccm, for example. In one embodiment, the PECVD process is implemented at the temperature of 400° C. and at the pressure of 5.5 torr. Here, the flow ratio of N₂O to SiH₄ is 0.57, a flow rate of N₂O and that of SiH₄ are 90 sccm and 168 sccm, respectively, and the high-frequency power provided through the implementation of the PECVD process is 120 W.

Thereafter, as shown in FIG. 3C, an upper-dielectric layer 108 is formed on the SSRO layer 106. A material of the upper-dielectric layer 108 is, for example, silicon oxide, and the upper-dielectric layer 108 is formed by performing a low pressure chemical vapor deposition (LPCVD) method, for example. In one embodiment, a thickness of the upper-dielectric layer 108 ranges from 70 angstroms to 110 angstroms.

Next, referring to FIG. 3D, a gate conductive layer 110 is formed on the upper-dielectric layer 108. In one embodiment, the gate conductive layer 110 is a doped polysilicon layer and is formed by adopting an in-situ operation in a chemical vapor deposition (CVD) process. In another embodiment, the gate conductive layer 110 is constructed by one doped polysilicon layer and a silicide layer. In addition, the gate conductive layer 110 is formed by firstly adopting the in-situ operation in a CVD process, such that the doped polysilicon layer is formed. Thereafter, another CVD process is performed for forming the silicide layer.

Afterwards, referring to FIG. 3E, a patterning process is carried out to form a patterned photoresist layer (not shown) on the gate conductive layer 110. In addition, a portion of the gate conductive layer 110, the upper-dielectric layer 108, the SSRO layer 106 and the tunneling dielectric layer 104 are removed with use of the patterned photoresist layer as a mask, such that a surface of the substrate is exposed by areas uncovered by the photoresist layer. Eternally, the photoresist layer is removed. A method for removing the portion of the gate conductive layer 110, the upper-dielectric layer 108, the SSRO layer 106 and the tunneling dielectric layer 104 is, for example, a dry etching method. On the other hand, a method of removing the photoresist layer is, for example, conducting a wet etching method with use of H₂SO₄ solution or the like to strip the photoresist layer.

According to the above embodiments, the doped regions serving as the source/drain are firstly formed, and a gate structure is subsequently constructed. However, the present invention is not limited thereto. The doped regions serving as the source/drain may also be formed after the formation of the gate structure.

FIG. 4 is a curve diagram illustrating a relation between a PGM time and a variation of a corresponding threshold voltage (ΔV_(T)) in a conventional silicon nitride device and that in a SSRO device according to the present invention.

A curve 400 represents a relation between the PGM time and the corresponding ΔV_(T) in the SSRO device (referring to as “device 1” hereinafter). The device 1 is constructed by a tunneling dielectric layer formed on a silicon substrate and having a thickness of 48 angstroms, a SSRO layer having a thickness of 100 angstroms and a refractive index at 248 nm wave length of _(—)1.7, a silicon oxide dielectric layer having a thickness of 90 angstroms, and a doped polysilicon gate. During the programming operation, a negative Fowler-Nordheim (−FN) programming is conducted by applying a −18V voltage to the doped polysilicon gate.

A curve 402 represents the relation between the PGM time and the corresponding ΔV_(T) in the conventional silicon nitride device (referring to as “device 2” hereinafter). The device 2 is constructed by the tunneling oxide layer formed on the silicon substrate and having the thickness of 48 angstroms, a silicon nitride layer having a thickness of 70 angstroms, the silicon oxide dielectric layer having the thickness of 90 angstroms, and the doped polysilicon gate. During the programming operation, the −FN programming is conducted by applying the −18V voltage to the doped polysilicon gate.

It is shown in FIG. 4 that as the −FN programming operations of the device 1 and the device 2 are conducted, ΔV_(T) of the device 1 is apparently larger than ΔV_(T) of the device 2 during a time period longer than 10⁻⁶ seconds but shorter than 10⁻² seconds. Moreover, it is indicated in FIG. 4 that during the −FN programming operations, a time required by the device 1 is obviously shorter than that required by the device 2 when the same ΔV_(T) (larger than 2V but smaller then 4V) is reached. Accordingly, the SSRO layer serving as the charge trapping layer in the present invention is capable of increasing both the number of the charges captured by the charge trapping layer and the capturing speed achieved thereby.

FIG. 5 is a curve diagram illustrating experimental results with respect to the relation between the PGM time and the corresponding ΔV_(T) in a silicon-rich oxide (SRO) device and that of a SSRO device according to the present invention.

A curve 500 represents the relation between the PGM time and the corresponding ΔV_(T) in the SSRO device (referring to as “device 3” hereinafter). The device 3 is constituted by the tunneling oxide layer formed on the silicon substrate and having the thickness of 48 angstroms, the SSRO layer having the thickness of 100 angstroms and the refractive index at 248 nm wave length of 1.7, the silicon oxide dielectric layer having the thickness of 90 angstroms, and the doped polysilicon gate. During the programming operation, the −FN programming is conducted by applying the −18V voltage to the doped polysilicon gate.

A curve 502 represents the relation between the PGM time and the corresponding ΔV_(T) in the SRO device (referring to as “device 4” hereinafter). The device 4 is constituted by the tunneling oxide layer formed on the silicon substrate and having the thickness of 48 angstroms, the SRO layer having the thickness of 100 angstroms and the refractive index at 248 nm wave length of 1.56, the silicon oxide dielectric layer having the thickness of 90 angstroms, and the doped polysilicon gate. During the programming operation, the −FN programming is conducted by applying the −18V voltage to the doped polysilicon gate.

It is shown in FIG. 5 that as the −FN programming operations of the device 3 and the device 4 are conducted, ΔV_(T) of the device 3 is apparently larger than ΔV_(T) of the device 4. Moreover, it is indicated in FIG. 5 that during the −FN programming operations, a time required by the device 3 is obviously shorter than that required by the device 4 when the same ΔV_(T) is reached.

To sum up, the SSRO layer is utilized as the charge trapping layer of the non-volatile memory cell in the present invention. Thereby, the number of the charges captured by the charge trapping layer can be increased, and the capturing speed achieved by the charge trapping layer can be raised.

It will be apparent to those skilled in the art that various modifications and variations can be made to the structure of the present invention without departing from the scope or spirit of the invention. In view of the foregoing, it is intended that the present invention cover modifications and variations of this invention provided they fall within the scope of the following claims and their equivalents. 

1. A fabricating method of a super-silicon-rich oxide (SSRO) non-volatile memory cell, comprising: forming a source/drain in a substrate; forming a tunneling dielectric layer on the substrate; implementing a plasma enhanced chemical vapor deposition (PECVD) process to form a SSRO layer serving as a charge trapping layer on the tunneling dielectric layer, wherein a reactive gas which is flowed during the implementation of the PECVD process comprises N₂O and SiH₄ having a flow ratio between 0.5 and 1 and a refractive index at 248 nm wave length of the SSRO layer ranges from 1.7 to 2 and a method of forming the SSRO layer comprises: forming a silicon oxide layer on the tunneling dielectric layer; and forming a plurality of cluster of silicon atoms in the silicon oxide layer; forming an upper-dielectric layer on the SSRO layer; and forming a gate conductive layer on the upper-dielectric layer.
 2. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a flow rate of N₂O during the implementation of the PECVD process ranges from 80 sccm to 100 sccm.
 3. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a flow rate of SiH₄ during the implementation of the PECVD process ranges from 160 to 180 sccm.
 4. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a temperature during the implementation of the PECVD process ranges from 350° C. to 450° C.
 5. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a pressure during the implementation of the PECVD process ranges from 2.5 torr to 8.5 torr.
 6. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a high-frequency power provided through the implementation of the PECVD process ranges from 100 W to 130 W.
 7. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a thickness of the SSRO layer ranges from 80 angstroms to 120 angstroms.
 8. The fabricating method of the SSRO non-volatile memory cell as claimed in claim 1, wherein a material of the upper-dielectric layer comprises silicon oxide.
 9. The cluster non-volatile memory cell as claimed in claim 1, wherein the step of forming the tunneling dielectric layer includes forming a tunneling oxide layer on the substrate.
 10. The cluster non-volatile memory cell as claimed in claim 1, wherein the step of forming the tunneling dielectric layer comprises forming a bottom oxide layer, a nitride layer and a top oxide layer from bottom to top formed on the substrate. 